3,067 research outputs found

    Integrative Analysis Frameworks for Improved Peptide and Protein Identifications from Tandem Mass Spectrometry Data.

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    Tandem mass spectrometry (MS/MS) followed by database search is the method of choice for high throughput protein identification in modern proteomic studies. Database searching methods employ spectral matching algorithms and statistical models to identify and quantify proteins in a sample. The major focus of these statistical methods is to assign probability scores to the identifications to distinguish between high confidence, reliable identifications that may be accepted (typically corresponding to a false discovery rate, FDR, of 1% or 5%) and lower confidence, spurious identifications that are rejected. These identification probabilities are determined, in general, considering only evidence from the MS/MS data. However, considering the wealth of external (orthogonal) data available for most biological systems, integrating such orthogonal information into proteomics analysis pipelines can be a promising approach to improve the sensitivity of these analysis pipelines and rescue true positive identifications that were rejected for want of sufficient evidence supporting their presence. In this dissertation, approaches based on naive bayes rescoring, search space restriction, and a hybrid approach that combines both are described for integrating orthogonal information in proteomic analysis pipelines. These methods have been applied for integrating transcript abundance data from RNA-seq and identification frequency data from the Global Proteome Machine database, GPMDB (one of the largest repositories of proteomic experiment results), into analysis pipelines, improving the number of peptide and protein identifications from MS/MS data. Further, estimation of false discovery rates in very large proteomic datasets was also investigated. In very large datasets, usually resulting from integrating data from multiple experiments, some assumptions used in typical target-decoy based FDR estimation in smaller datasets no longer hold true, resulting in artificially inflated error rates. Alternative approaches that would allow accurate FDR estimation in these large scale datasets have been described and benchmarked.PHDBioinformaticsUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://deepblue.lib.umich.edu/bitstream/2027.42/116717/1/avinashs_1.pd

    A nested mixture model for protein identification using mass spectrometry

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    Mass spectrometry provides a high-throughput way to identify proteins in biological samples. In a typical experiment, proteins in a sample are first broken into their constituent peptides. The resulting mixture of peptides is then subjected to mass spectrometry, which generates thousands of spectra, each characteristic of its generating peptide. Here we consider the problem of inferring, from these spectra, which proteins and peptides are present in the sample. We develop a statistical approach to the problem, based on a nested mixture model. In contrast to commonly used two-stage approaches, this model provides a one-stage solution that simultaneously identifies which proteins are present, and which peptides are correctly identified. In this way our model incorporates the evidence feedback between proteins and their constituent peptides. Using simulated data and a yeast data set, we compare and contrast our method with existing widely used approaches (PeptideProphet/ProteinProphet) and with a recently published new approach, HSM. For peptide identification, our single-stage approach yields consistently more accurate results. For protein identification the methods have similar accuracy in most settings, although we exhibit some scenarios in which the existing methods perform poorly.Comment: Published in at http://dx.doi.org/10.1214/09-AOAS316 the Annals of Applied Statistics (http://www.imstat.org/aoas/) by the Institute of Mathematical Statistics (http://www.imstat.org

    A statistical model-building perspective to identification of MS/MS spectra with PeptideProphet

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    Abstract PeptideProphet is a post-processing algorithm designed to evaluate the confidence in identifications of MS/MS spectra returned by a database search. In this manuscript we describe the "what and how" of PeptideProphet in a manner aimed at statisticians and life scientists who would like to gain a more in-depth understanding of the underlying statistical modeling. The theory and rationale behind the mixture-modeling approach taken by PeptideProphet is discussed from a statistical model-building perspective followed by a description of how a model can be used to express confidence in the identification of individual peptides or sets of peptides. We also demonstrate how to evaluate the quality of model fit and select an appropriate model from several available alternatives. We illustrate the use of PeptideProphet in association with the Trans-Proteomic Pipeline, a free suite of software used for protein identification.http://deepblue.lib.umich.edu/bitstream/2027.42/112836/1/12859_2012_Article_5421.pd

    Evaluating the effect of database inflation in proteogenomic search on sensitive and reliable peptide identification

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    Comparison of novel peptides identified from real proteogenomic databases. (DOCX 68 kb
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